Division of Nephrology, Department of Clinical Sciences, Lund University, University Hospital, Malmö, Sweden.
BJU Int. 2011 Jun;107(11):1769-74. doi: 10.1111/j.1464-410X.2010.09761.x. Epub 2010 Oct 18.
Diagnostic (exploratory cohort).
2b.
To assess variation of total prostate-specific antigen (tPSA), free PSA (fPSA), percent fPSA, human glandular kallikrein 2 (hK2) and intact PSA measured three times within 2 weeks. Knowledge of the variation in an individual's PSA level is important for clinical decision-making.
Study participants were 149 patients referred for prostate biopsy, of which 97 had benign disease and 52 had prostate cancer. Three blood samples were drawn with a median of 4 h between first and second samples and 12 days between first and third samples. Variability was described by absolute differences, ratios and intra-individual coefficients of variation. Total PSA, fPSA, hK2 and intact PSA were measured in anticoagulated blood plasma.
At baseline, the median tPSA was 6.8 (interquartile range, 4.5-9.6) ng/mL. The intra-individual variation was low for all biomarkers, and lowest for tPSA. For 80% of participants, the ratio between first and second time points for tPSA was in the range 0.91-1.09 and the ratio for percent fPSA was in the range 0.89-1.15. Total coefficients of variation between time 1 and 2 for tPSA, fPSA, percent fPSA, hK2 and intact PSA were 4.0%, 6.6%, 6.0%, 9.2% and 9.5%, respectively. The measurements taken several days apart varied more than those taken on the same day, although the variation between both time points was not large.
The intra-individual variation for all the kallikrein-like markers studied was relatively small, especially for samples drawn the same day. Few cases are reclassified between the time points. This indicates the high short-term biological and technical reproducibility of the tests in clinical use.
诊断(探索性队列)。
2b。
评估在 2 周内采集 3 次的总前列腺特异性抗原(tPSA)、游离前列腺特异性抗原(fPSA)、fPSA 百分比、人组织激肽释放酶 2(hK2)和完整 PSA 的变化。了解个体 PSA 水平的变化对临床决策很重要。
本研究纳入 149 例因前列腺活检而就诊的患者,其中 97 例为良性疾病,52 例为前列腺癌。两次采血的中位时间间隔为 4 小时,第一次和第三次采血的时间间隔为 12 天。通过绝对差异、比值和个体内变异系数来描述变异性。在抗凝血浆中测量总 PSA、fPSA、hK2 和完整 PSA。
基线时,中位 tPSA 为 6.8(四分位间距,4.5-9.6)ng/ml。所有生物标志物的个体内变异性均较低,tPSA 最低。对于 80%的参与者,tPSA 第一次和第二次检测结果的比值在 0.91-1.09 范围内,fPSA 百分比的比值在 0.89-1.15 范围内。tPSA、fPSA、fPSA 百分比、hK2 和完整 PSA 从时间点 1 到时间点 2 的总变异系数分别为 4.0%、6.6%、6.0%、9.2%和 9.5%。相隔数天的测量结果变化大于同一天的测量结果变化,尽管两次测量之间的变化不大。
在所研究的所有激肽样标志物中,个体内变异性相对较小,尤其是同一天采集的样本。在不同时间点之间重新分类的情况很少。这表明在临床应用中,这些检测具有较高的短期生物学和技术重复性。